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Wei Yin
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EP1.11 - Screening and Early Detection (ID 201)
- Event: WCLC 2019
- Type: E-Poster Viewing in the Exhibit Hall
- Track: Screening and Early Detection
- Presentations: 1
- Moderators:
- Coordinates: 9/08/2019, 08:00 - 18:00, Exhibit Hall
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EP1.11-07 - Development of a Chromosome Instabilities in Plasma Cell-Free DNA Assay for Early Lung Cancer Detection and Treatment Response Monitoring (ID 2126)
08:00 - 18:00 | Author(s): Wei Yin
- Abstract
Background
Background: Chromosomal instability (CIN) is one of the hallmarks of cancer. Tumor cells keep shedding DNA into blood stream which provides an opportunity for CIN analysis. Here we present a retrospective study to investigate the potential of CIN in plasma cell-free DNA (cfDNA) as a minimal-invasive biomarker for early cancer detection and cancer treatment responses monitoring.
Method
Methods: To characterization the baseline data of CIN in cfDNA, 171 plasma samples were collected since June 2017. 35 was from non-cancer individuals. 136 was from cancer patients. cfDNA was extracted and sent to low-coverage genome sequencing on the Illumina X10 platform, followed by chromosomal instability (CIN) analyses by a customized workflow Ultrasensitive Chromosomal Instability Detector (UCAD).
Result
Results:
Increased plasma cfDNA CIN was observed along with disease progression. In lung cancer, cfDNA CIN increased along with the development of lesions, from adenocarcinoma in-situ, minimal invasive adenocarcinoma, invasive adenocarcinoma (P=0.034) to relapsed cancer (P<0.01). The sensitivity of early lung cancer detection was 30.7%, 37.5%, 45.5%, 50.0% and 98.1% for AIS, MIA, IAC, SCC and relapsed lung cancer, at a specificity of 75%.
In primary lung cancer, cfDNA CIN decreased after curative therapies. And cfDNA CIN significantly increased after disease relapsed (P<0.01). And cfDNA levels did not show statistical differences regarding metastases sites.
Conclusion
Conclusions:
cfDNA CIN can help early cancer detection and treatment response monitoring.